FDA 510(k)

SUREcore Prime Biopsy Instrument

Número K: K230646 · 2023-11-29

Data da decisão2023-11-29

Código do produtoKNW

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

SUREcore Prime Biopsy Instrument is the device name listed in this FDA 510(k) record. The listed applicant is Uro-1 Medical, Inc.. It received FDA 510(k) clearance on 2023-11-29 under 510(k) number K230646. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the SUREcore Prime Biopsy Instrument?

SUREcore Prime Biopsy Instrument is a medical device that received FDA 510(k) clearance on 2023-11-29. The listed applicant is Uro-1 Medical, Inc.. The 510(k) number is K230646.

When did SUREcore Prime Biopsy Instrument receive FDA 510(k) clearance?

SUREcore Prime Biopsy Instrument received FDA 510(k) clearance on 2023-11-29, under 510(k) number K230646.

Who is the listed applicant for SUREcore Prime Biopsy Instrument?

The FDA 510(k) record lists Uro-1 Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUREcore Prime Biopsy Instrument?

The FDA product code for SUREcore Prime Biopsy Instrument is KNW.

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